Gunnar Houge
Gunnar Houge
Professor, Dep med genetics, Haukeland University Hospital
Verified email at helse-bergen.no
Title
Cited by
Cited by
Year
Formation of new chromatin domains determines pathogenicity of genomic duplications
M Franke, DM Ibrahim, G Andrey, W Schwarzer, V Heinrich, R Schöpflin, ...
Nature 538 (7624), 265-269, 2016
4132016
The protein phosphatase inhibitor okadaic acid induces morphological changes typical of apoptosis in mammalian cells
R Bøe, BT Gjertsen, OK Vintermyr, G Houge, M Lanotte, SO Døskeland
Experimental cell research 195 (1), 237-246, 1991
3971991
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia …
F Pasutto, H Sticht, G Hammersen, G Gillessen-Kaesbach, DR FitzPatrick, ...
The American Journal of Human Genetics 80 (3), 550-560, 2007
3242007
Fabry disease: overall effects of agalsidase alfa treatment
M Beck, R Ricci, U Widmer, F Dehout, AG De Lorenzo, C Kampmann, ...
European journal of clinical investigation 34 (12), 838-844, 2004
2682004
Treatment of Fabry disease: outcome of a comparative trial with agalsidase alfa or beta at a dose of 0.2 mg/kg
AC Vedder, GE Linthorst, G Houge, JEM Groener, EE Ormel, BJ Bouma, ...
PloS one 2 (7), e598, 2007
2392007
Agalsidase benefits renal histology in young patients with Fabry disease
C Tøndel, L Bostad, KK Larsen, A Hirth, BE Vikse, G Houge, E Svarstad
Journal of the American Society of Nephrology 24 (1), 137-148, 2013
2232013
CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta
D Baldridge, U Schwarze, R Morello, J Lennington, TK Bertin, JM Pace, ...
Human mutation 29 (12), 1435-1442, 2008
2192008
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
BH Anderson, PR Kasher, J Mayer, M Szynkiewicz, EM Jenkinson, ...
Nature genetics 44 (3), 338-342, 2012
2102012
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype
T Kleefstra, WA van Zelst-Stams, WM Nillesen, V Cormier-Daire, G Houge, ...
Journal of medical genetics 46 (9), 598-606, 2009
1812009
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
B Coste, G Houge, MF Murray, N Stitziel, M Bandell, MA Giovanni, ...
Proceedings of the National Academy of Sciences 110 (12), 4667-4672, 2013
1732013
A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
D Wieczorek, N Bögershausen, F Beleggia, S Steiner-Haldenstätt, E Pohl, ...
Human molecular genetics 22 (25), 5121-5135, 2013
1612013
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development
S Benko, CT Gordon, D Mallet, R Sreenivasan, C Thauvin-Robinet, ...
Journal of medical genetics 48 (12), 825-830, 2011
1552011
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
S Banka, R Veeramachaneni, W Reardon, E Howard, S Bunstone, ...
European Journal of Human Genetics 20 (4), 381-388, 2012
1422012
Programmed cell death (apoptosis) is induced rapidly and with positive cooperativity by activation of cyclic adenosine monophosphate‐kinase I in a myeloid leukemia cell line
M Lanotte, JB Riviere, S Hermouet, G Houge, OK Vintermyr, BT Gjertsen, ...
Journal of cellular physiology 146 (1), 73-80, 1991
1361991
Fine mapping of 28S rRNA sites specifically cleaved in cells undergoing apoptosis
G Houge, B Robaye, TS Eikhom, J Golstein, G Mellgren, BT Gjertsen, ...
Molecular and Cellular Biology 15 (4), 2051-2062, 1995
1331995
Update on Kleefstra syndrome
MH Willemsen, AT Vulto-van Silfhout, WM Nillesen, WM Wissink-Lindhout, ...
Molecular syndromology 2 (3-5), 202-212, 2011
1322011
Two distinctly regulated events, priming and triggering, during retinoid-induced maturation and resistance of NB4 promyelocytic leukemia cell line
S Ruchaud, E Duprez, MC Gendron, G Houge, HG Genieser, B Jastorff, ...
Proceedings of the National Academy of Sciences 91 (18), 8428-8432, 1994
1321994
Multiple apoptotic death types triggered through activation of separate pathways by cAMP and inhibitors of protein phosphatases in one (IPC leukemia) cell line
BT Gjertsen, LI Cressey, S Ruchaud, G Houge, M Lanotte, SO Doskeland
Journal of cell science 107 (12), 3363-3377, 1994
1151994
Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are risk factors for colorectal cancer
RM de Voer, AG van Kessel, RDA Weren, MJL Ligtenberg, D Smeets, ...
Gastroenterology 145 (3), 544-547, 2013
982013
A retinoid acid'resistant't (15; 17) acute promyelocytic leukemia cell line: isolation, morphological, immunological, and molecular features.
E Duprez, S Ruchaud, G Houge, V Martin-Thouvenin, F Valensi, ...
Leukemia 6 (12), 1281-1287, 1992
971992
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